Color-photographic recording material

ABSTRACT

A color-photographic recording material is described which contains a magenta coupler and, as stabilizer, at least one compound of the formula ##STR1## where the radicals are as defined in claim 1.

The present invention relates to a novel colour-photographic recording material which contains a magenta coupler and, as light stabilizer, a hydroxyalkyl hydroquinone ether.

The alkylated hydroquinone ethers or diethers used hitherto as stabilizers in photographic materials exhibited inadequate activity, in particular in the case of 1H-pyrazolo-[5,1-c][1,2,4]triazole magenta couplers (see also structure C-5). The photostability of the magenta dyes was inadequate. In addition, the colour couplers had hitherto to be predissolved in high-boiling oils before they could be dispersed in the gelatin. Although some known stabilizers would in principle have been suitable as coupler oils, they have side effects, for example sensitometric effects, wavelength shifts of the dye absorption, or yellowing on weathering or in an Atlas tester, and were therefore unsatisfactory.

A group of hydroxyalkyl hydroquinone ethers has now been found which, surprisingly, has proved substantially free from such disadvantages. In addition, they are also suitable as coupler oils and thus facilitate a simplified incorporation of the couplers. In particular, this group of hydroquinones is suitable for increasing the stability of magenta dyes in colour-photographic materials.

The novel stabilizers can be used for all types of photosensitive materials. For example, they can be employed for colour paper, colour reversal paper, direct-positive colour material, colour negative film, colour positive film, colour reversal film, etc. They are preferably used, inter alia, for photosensitive colour material which contains a reversal substrate or forms positives.

Colour-photographic recording materials usually contain, on a support, a blue-sensitive and/or a green-sensitive and/or a red-sensitive silver-halide emulsion layer and, if desired, a protection layer, the stabilizer for the magenta dye being in the green-sensitive layer.

The present application thus relates to a colour-photographic recording material which contains a magenta coupler and, as stabilizer, at least one compound of the formula ##STR2## where R₁ and R₃, independently of one another, are hydrogen, C₁ -C₁₂ alkyl, C₅ -C₇ cycloalkyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl groups, or are phenyl-C₁ -C₄ alkyl, phenyl, C₁ -C₈ alkoxy or a group of the formula V ##STR3## in which R₈ and R₉, independently of one another, are C₁ -C₈ alkyl;

n is 1-10, and R₁₀ is hydrogen, C₁ -C₂₄ alkyl, which is unsubstituted or interrupted by one or more --O-- atoms and is unsubstituted or substituted by one --OH group, or is C₂ -C₁₈ alkenyl, C₅ -C₁₂ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₄ alkyl, or is phenyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl, or is phenyl-C₁ -C₄ alkyl or furfuryl;

R₂ and R₄, independently of one another, are hydrogen or C₁ -C₁₂ alkyl;

R₅ is hydrogen, --CO--R₁₁, --CO--OR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl; R₁₂ is C₁ -C₄ alkyl and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl or phenyl; the radicals R₆, independently of one another, are --OR₁₆ or C₁ -C₁₅ alkyl, in which R₁₆ is hydrogen, C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl, phenyl-C₁ -C₄ alkyl, C₃ C₂₄ alkyl or C₂ -C₁₄ hydroxyalkyl, each of which is interrupted by one or more O atoms, or is phenyl, which is unsubstituted or substituted by C₁ -C₄ alkyl, C₁ -C₄ alkoxy or halogen, tolyl, C₅ -C₆ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₈ alkyl, or is -- CO--R₁₁, in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl;

R₇ is hydrogen, C₁ -C₁₂ alkyl, which is uninterrupted or interrupted by one or more --O--, --S-- or --SO₂ -- groups, C₅ -C₁₂ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₄ alkyl, or is phenyl-C₁ -C₄ alkyl, a group of the formula VI ##STR4## or a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ and R₆ are as defined for formula I,

R₁₇ is hydrogen or C₁ -C₁₈ alkyl, and R₁₈ is C₁ -C₁₂ alkyl, which is unsubstituted or interrupted by one or more --O-- atoms, or is C₂ -C₁₈ alkenyl, benzyl or phenyl, which is unsubstituted or substituted by 1-3 C₁ -C₄ alkyl;

R₁₉ is C₂ -C₁₀ alkylene, phenylene or a-phenylene-R₂₀ -phenylene- group, in which R₂₀ is --O--, --S--, --SO₂ --, --CH₂ -- or --C(CH₃)₂ ;

m is 1-100;

A₁ is hydrogen, --CH₂ CH(OR₅)CH₂ OR₁₉ OCH(OR₅)CH₂ OR₅ or ##STR5## and A₂ is --OH or ##STR6## or R₃ and R₇ in the formula I, together with the atoms to which they are bonded, form a C₅ -C₆ ring, which is unsubstituted or substituted by 1 to 3 C₁ -C₈ alkyl.

Any C₁ -C₂₄ alkyl substitutents in the compounds according to the invention are radicals such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tetradecyl, hexadecyl and octadecyl, and corresponding branched isomers.

C₅ -C₁₂ cycloalkyl radicals are, for example, cyclopentyl, cyclohexyl, cyclooctyl or cyclododecyl.

Alkyl radicals having 3 to 24 carbon atoms which are interrupted by oxygen are, for example, --(CH₂ CH₂ O)₁₋₁₁ CH₃ and --(CH₂ CH₂ O)₁₋₁₁ CH₂ CH₃.

Alkenyl radicals having 2 to 18 carbon atoms may be monounsaturated or, from 4 carbon atoms, polyunsaturated.

Alkylene radicals having 2 to 10 carbon atoms can be derived from corresponding alkyl radicals.

C₁ -C₈ alkoxy radicals are, for example, methoxy, ethoxy, propoxy, butoxy or hexoxy and corresponding branched isomers.

Preference is given to stabilizers of the formula ##STR7## in which R₁ and R₃, independently of one another, are hydrogen, C₁ -C₈ alkyl, cyclohexyl, --C(CH₃)₂ C₆ H₅, C₁ -C₄ alkoxy or a group of the formula V ##STR8## in which R₈ and R₉ are methyl; n is 3, and

R₁₀ is hydrogen, C₁ -C₁₂ alkyl, which is unsubstituted or interrupted by one or more --O-- atoms and is unsubstituted or substituted by one --OH, or is C₂ -C₁₈ alkenyl or benzyl;

R₂ is hydrogen;

R₄ is hydrogen or C₁ -C₈ alkyl;

R₅ is hydrogen,--CO--R₁₁, --CO--OR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl, R₁₂ is C₁ -C₄ alkyl, and

R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl or phenyl; the radicals R₆ independently of one another, are --OR₁₆, in which

R₁₆ is hydrogen, C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl, phenyl-C₁ -C₄ alkyl, C₃ -C₂₄ alkyl or C₂ -C₁₄ hydroxyalkyl, each of which is interrupted by one or more O atoms, or is phenyl, tolyl, C₅ -C₆ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₈ alkyl, or is --CO--R₁₁, in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl; R₇ is C₁ -C₄ alkyl, a group of the formula VI ##STR9## or a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ and R₆ are as defined for formula I,

R₁₇ is hydrogen or C₁ -C₁₂ alkyl, and R₁₈ is C₁ -C₈ alkyl;

R₁₉ is C₂ -C₈ alkylene, phenylene or a -phenylene-R₂₀ -phenylene- group, in which R₂₀ is --SO₂ --, --CH₂ -- or --C(CH₃)₂ --;

m is 1-50;

A₁ is hydrogen, --CH₂ CH(OR₅)CH₂ OR₁₉ OCH(OR₅)CH₂ OR₅ or ##STR10## and ##STR11## Particular preference is given to stabilizers of the formulae ##STR12## in which R₁ and R₃, independently of one another, are hydrogen, C₁ -C₈ alkyl, C₁ -C₄ alkoxy or a group of the formula V ##STR13## in which R₈ and R₉ are methyl, n is 3, and

R₁₀ is C₁ -C₄ alkyl;

R₂ is hydrogen;

R₄ is hydrogen or C₁ -C₈ alkyl;

R₅ is hydrogen, --CO--R₁₁, --COOR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₄ alkyl or C₂ -C₃ alkenyl, R₁₂ is C₁ -C₄ alkyl, and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl; the radicals R₆, independently of one another, are --OR₁₆, in which R₁₆ is C₁ -C₁₈ alkyl, allyl, benzyl, phenyl, C₃ -C₁₂ alkyl which is interrupted by one or more O atoms, or is cyclohexyl or --CO--R₁₁, in which R₁₁ is C₁ -C₄ alkyl or C₂ -C₃ alkenyl;

R₇ is a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ and R₆ are as defined for formula I;

R₁₉ is C₂ -C₈ alkylene or a phenylene-R₂₀ -phenylene- group, in which R₂₀ is --C(CH₃)₂ --;

m is 1-25;

A₁ is hydrogen, --CH₂ CH(OR₅)CH₂ OR₁₉ OCH(OR₅)CH₂ OR₅ or ##STR14## and A₂ is --OH or ##STR15##

Of particular significance are stabilizers of the formula ##STR16## in which R₁, R₃ and R₄, independently of one another, are hydrogen or C₁ -C₈ alkyl;

R₂ is hydrogen;

R₅ is hydrogen or --CO--CH₃ ;

R₁₆ is C₁ -C₁₂ alkyl, allyl or C₃ -C₇ alkyl which is interrupted by 1-3 O atoms; and

R₇ is a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ is as defined for formula I and R₆ is --OR₁₆.

Very particular preference is given to stabilizers of the formula ##STR17## in which R₁, R₃ and R₄, independently of one another, are hydrogen or C₁ -C₈ alkyl;

R₂ is hydrogen;

R₅ is hydrogen;

R₁₆ is C₁ -C₁₂ alkyl, and

R₇ is a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ is as defined for formula 1 and R₆ is --OR₁₆.

The novel material preferably contains gelatin interlayers between the silver-halide emulsion layers.

Preference is given to photographic materials of this type in which the silver-halide in the blue-sensitive and/or green-sensitive and/or red-sensitive layer is silver chloride bromide comprising at least 90 mol % of silver chloride.

Preference is furthermore given to photographic materials which contain the silver-halide emulsion layers in the sequence blue-sensitive, green-sensitive and red-sensitive layers.

Typical and preferred stabilizers according to the invention are the following:

    __________________________________________________________________________     Examples                                                                       __________________________________________________________________________      ##STR18##                                                                     No.                                                                               R.sub.1       R.sub.3        R.sub.4                                                                            R.sub.7                                    __________________________________________________________________________      1.                                                                               C(CH.sub.3).sub.3                                                                            C(CH.sub.3).sub.3                                                                             H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                     2.                                                                               C(CH.sub.3).sub.3                                                                            C(CH.sub.3).sub.3                                                                             H   H                                           3.                                                                               OC.sub.4 H.sub.9                                                                             OC.sub.4 H.sub.9                                                                              H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                     4.                                                                               OC.sub.4 H.sub.9                                                                             OC.sub.4 H.sub.9                                                                              H   H                                           5.                                                                               C(CH.sub.3).sub.2 (CH.sub.2).sub.3 COOCH.sub.3                                               C(CH.sub.3).sub.2 (CH.sub.2).sub.3 COOCH.sub.3                                                H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                     6.                                                                               C(CH.sub.3).sub.2 (CH.sub.2).sub.3 COOCH.sub.3                                               C(CH.sub.3).sub.2 (CH.sub.2).sub.3 COOCH.sub.3                                                H   H                                           7.                                                                               C(CH.sub.3).sub.2 CH.sub.2 C(CH.sub.3).sub.3                                                 H              H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub. 9                                    8.                                                                               H             C(CH.sub.3).sub.2 CH.sub.2 C(CH.sub.3).sub.3                                                  H   H                                           9.                                                                               C(CH.sub.3).sub.2 CH.sub.2 C(CH.sub.3).sub.3                                                 C(CH.sub.3).sub.2 CH.sub.2 C(CH.sub.3).sub.3                                                  H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                    10.                                                                               C(CH.sub.3).sub.2 CH.sub.2 C(CH.sub.3).sub.3                                                 C(CH.sub.3).sub.2 CH.sub.2 C(CH.sub.3).sub.3                                                  H   H                                             C(CH.sub.3).sub.3                                                                            H              H   CH.sub.2 (CH.sub.12 H.sub.25)COOC.sub.                                         2 H.sub.5                                     H             H              H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                       CH.sub.3      CH.sub.3       CH.sub.3                                                                           CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                       CH.sub.3      CH.sub.3       H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                       H             C(CH.sub.3)3   H   H                                             CH.sub.3      H              H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                       H             H              H   C.sub.12 H.sub.25                             CH.sub.3      CH.sub.3       H   C.sub.12 H.sub.25                             H             CH.sub.3       CH.sub.3                                                                           CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                    20.                                                                               C(CH.sub.3).sub.3                                                                            H              H   CH.sub.2 CH(OH)CH.sub.2 OC.sub.4                                               H.sub.9                                    __________________________________________________________________________      ##STR19##                                                                     No.                                                                               R.sub.1                                                                             R.sub.3                                                                             R.sub.5           R.sub.16 = R.sub.16 '                           __________________________________________________________________________     21 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   H                 CH.sub.2 CH.sub.2 OCH.sub.3                     22 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   COCH.sub.3        CH.sub.2 CH.sub.2 OCOCH.sub.3                   23 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   COCH.sub.3        CH.sub.2 CH.sub.2 OCH.sub.3                     24 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   COCH.sub.3        C.sub.4 H.sub.9                                 25 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   COC.sub.4 H.sub.9 C.sub.4 H.sub.9                                 26 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   COCH.sub.3        COCH.sub.3                                      27 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   Si(CH.sub.3).sub.2 [C(CH.sub.3).sub.2 CH(CH.sub.3).sub.2                                         C.sub.4 H.sub.9                                 28 C(CH.sub.3).sub.3                                                                   H    H                 H                                               29 CH.sub.3                                                                            H    H                 H                                               30 CH.sub.3                                                                            CH.sub.3                                                                            H                 H                                               31 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   H                 CH.sub.2 CH(OH)CH.sub.2 OCH.sub.2 CH(C.sub.                                    2 H.sub.5)C.sub.4 H.sub.9                       32 C(CH.sub.3).sub.3                                                                   C(CH.sub.3).sub.3                                                                   H                 CH.sub.2 CH.sub.2 OH                            __________________________________________________________________________     No.  R.sub.1  R.sub.3   R.sub.5                                                                               R.sub.16 /R.sub.16 '                            __________________________________________________________________________     32/a CH.sub.3 H         H      CH.sub.2 CH(C.sub.2 H.sub.5)C.sub.4                                            H.sub.9                                         32/b CH.sub.3 CH.sub.3  H      CH.sub.2 CH(C.sub.2 H.sub.5)C.sub.4                                            H.sub.9                                         32/c CH.sub.3 H         H                                                                                      ##STR20##                                      32/d CH.sub.3 H         H      CH(CH.sub.3).sub.2                              32/e CH.sub.3 H         H      CH.sub.2 CHCH.sub.2                             32/f CH.sub.3 H         H      CH.sub.2 CH(CH.sub.3).sub.2                     32/g CH.sub.3 CH.sub.3  H      CH(CH.sub.3).sub.2                              32/h CH.sub.3 H         H                                                                                      ##STR21##                                      32/i CH.sub.3 H         H      C(CH.sub.3).sub.3                               32/j CH.sub.3 H         H      Cyclohexyl                                      32/k C(CH.sub.3).sub.3                                                                       C(CH.sub.3).sub.3                                                                        H                                                                                      ##STR22##                                      32/l CH.sub.3 CH.sub.3  COCH.sub.3                                                                            C.sub.4 H.sub.9                                 32/m CH.sub.3 H         CH.sub.3                                                                              C.sub.4 H.sub.9                                 32/n CH.sub.3 CH.sub.3  CH.sub.3                                                                              C.sub.4 H.sub.9                                 33   CH.sub.3 CH.sub.3  H      C.sub.4 H.sub.9 /CH.sub.2 (C.sub.2                                             H.sub.5)C.sub.4 H.sub.9                         34   CH.sub.3 CH.sub.3  H      C(CH.sub.3).sub.3 /C.sub.4 H.sub.9              35   C(CH.sub.3).sub.3                                                                       C(CH.sub.3).sub.3                                                                        H      CH.sub.2 CH(C.sub.2 H.sub.5)C.sub.4                                            H.sub.9 /C(CH.sub.3).sub.3                      36   C(CH.sub.3).sub.3                                                                       C(CH.sub.3).sub.3                                                                        H      CH.sub.2 CH(CH.sub.3).sub.2 /C(CH.sub.3).su                                    b.3                                             37   CH.sub.3 CH.sub.3  H      CH.sub.2 CH(CH.sub.3).sub.2 /C(CH.sub.3).su                                    b.3                                             38   CH.sub.3 CH        H      CH.sub.2 CH(CH.sub.3).sub.2 /C.sub.4                                           H.sub.9                                         39   CH.sub.3 H         H      CH.sub.2 CH(CH.sub.3).sub.2 /C.sub.4                                           H.sub.9                                         40   CH.sub.3 H         H      CH.sub.2 CH(CH.sub.3).sub.2 /CH.sub.2                                          CH.sub.2 CH(CH.sub.3).sub.2                     41   C(CH.sub.3).sub.3                                                                       H         H      CH.sub.2 CH(CH.sub.3).sub.2 /C.sub.6                                           H.sub.5                                         41/a C(CH.sub.3).sub.2 C.sub.2 H.sub.5                                                       C(CH.sub.3).sub.2 C.sub.2 H.sub.5                                                        H      C(CH.sub.3).sub.3 /C.sub.4 H.sub.9              41/b CH.sub.3 CH.sub.3  H      (CH.sub.2 CH.sub.2 O)CH.sub.3 /(CH.sub.2                                       CH.sub.2 O).sub.2 C.sub.2 H.sub.5               41/c CH.sub.3 CH.sub.3  H      C(CH.sub.3).sub.3 /C.sub.4 H.sub.9              41/d CH.sub.3 CH.sub.3  H      C.sub.5 H.sub.11 /CH.sub.2 CH.sub.2                                            CH(CH.sub.3).sub.2                              41/e CH.sub.3 H         H      C(CH.sub.3).sub.3 /C.sub.4 H.sub.9              41/f CH.sub.3 CH.sub.3  H      C.sub.12 H.sub.25 /C.sub.13 H.sub.27                                           /C.sub.14 H.sub.29                              41/g C(CH.sub.3).sub.3                                                                       H         H      C.sub.6 H.sub.4OCH.sub.3 (para)                 41/h C(CH.sub.3).sub.3                                                                       C(CH.sub.3).sub.3                                                                        H      C.sub.6 H.sub.4OCH.sub.3 (para)                 41/i CH.sub.3 H         H      C.sub.6 H.sub.4OCH.sub.3 (para)                 41/j H        H         H      C.sub.6 H.sub.4OCH.sub.3 (para)                 41/k C(CH.sub.3).sub.3                                                                       C(CH.sub.3).sub.3                                                                        H      C.sub.6 H.sub.5                                 41/l C(CH.sub.3).sub.3                                                                       H         H      C.sub.6 H.sub.5                                 41/m C(CH.sub.3).sub.3                                                                       H         H      C.sub.6 H.sub.5                                 42                                                                                 ##STR23##                                                                  43                                                                                 ##STR24##                                                                  __________________________________________________________________________      ##STR25##                                                                     No.                                                                               R                                                                           __________________________________________________________________________     44 CH.sub.2 CH(OH)CH.sub.2 OC.sub.4 H.sub.9                                    45 CH.sub.2 CH(OH)CH.sub.2 OCH.sub.2 CH(C.sub.2H.sub.5)C.sub.4 H.sub.9         46 CH.sub.2 CH(OH)CH.sub.2 OC.sub.13 H.sub.27 (C.sub.15 H.sub.31)              47                                                                                 ##STR26##                                                                      ##STR27##                                                                  48 R.sub.16 = R.sub.16 ' = C.sub.4 H.sub.9                                     49 R.sub.16 = R.sub.16 ' = CH.sub.2 CH(C.sub.2 H.sub.5)C.sub.4 H.sub.9         50                                                                                 ##STR28##                                                                  __________________________________________________________________________

Usually the stabilizers according to the present invention are employed in a 0.1 to 4-fold, preferably 0.2 to 2-fold, amount by weight, based on the conjointly used color coupler.

The magenta couplers in the colour-photographic recording material can be, for example, simple 1-aryl-5-pyrazolones or pyrazole derivatives which are fused to 5-membered heterocyclic rings, e.g. imidazopyrazoles, pyrazolopyrazoles, pyrazolotriazoles or pyrazolotetrazoles.

A group of magenta couplers comprises 5-pyrazolones of the formula C ##STR29## as described in British Patent 2 003 473. In this formula, R₁₆ is hydrogen, alkyl, aryl, alkenyl or a heterocyclic group. R₁₇ is hydrogen, alkyl, aryl, a heterocyclic group, an ester group, an alkoxy group, an akkylthio group, a carboxyl group, an arylamino group, an acylamino group, a (thio)urea group, a (thio)carbamoyl group, a guanidino group or a sulfonamido group.

R₁₇ is preferably a ##STR30## group, in which R₁₈ is imino, acylamino or ureido, R₁₉ is hydrogen, halogen, alkyl or alkoxy, R₂₀ is hydrogen, alkyl, acylamino, carbamoyl, sulfamoyl, sulfonamido, alkoxycarbonyl, acyloxy or a urethane group.

If Q' is hydrogen, the magenta coupler is tetraequivalent with respect to the silver-halide.

Preferred examples of magenta couplers of this type are compounds of the formula ##STR31## in which R₂₀ is as defined above, and Q', as described above, is a leaving group. These compounds are preferably present in the material according to the invention.

Further examples of tetraequivalent magenta couplers of this type are given in U.S. Pat. Nos. 2,983,608, 3,061,432, 3,062,653, 3,127,269, 3,152 896, 3,311,476, 3,419,391, 3,519429, 3,558,319, 3,582,322, 3,615,506, 3,684,514, 3,834,908, 3,888,680, 3,891,445, 3,907,571, 3,928,044, 3,930,861, 3,930,866 and 3,933,500 and JP-A89/309 058.

If Q' in the formula C is not hydrogen, but instead a group which is eliminated during the reaction with the oxidized developer, the magenta coupler is diequivalent. In this case, Q can be, for example, halogen or a group bonded to the pyrazole ring via O, S or N. Diequivalent couplers of this type give greater colour density and are more reactive towards the oxidized developer than are the corresponding tetraequivalent magenta couplers.

Examples of diequivalent magenta couplers are described in U.S. Pat. Nos. 3,006,579, 3,419,391, 3,311,476, 3,432,521, 3,214,437, 4,032,346, 3,701,783, 4,351,897, 3,227,554, in EP-A 133 503, DE-A 2 944 601, JP-A 78/34 044, 74/53 435, 74/53 436, 75/53 372 and 5/122 935.

Typical and preferred magenta couplers conform to the formulae: ##STR32##

It is possible for 2 pyrazolone rings to be linked via a divalent Q', giving so-called bis-couplers. These are described, for example, in U.S. Pat. No. 2,632,702, U.S. Pat. No. 2,618,864, GB-A 968 461, GB-A 786 859, JP-A 76/37 646, 59/4086, 69/16 110, 69/26 589, 74/37 854 and 74/29 638. Y is preferably an O-alkoxyarylthio group.

As mentioned above, the magenta couplers used can also be pyrazoles fused to 5-membered heterocyclic tings, known as pyrazoloazoles. Their advantages over simple pyrazoles are that they give dyes of greater formalin resistance and have purer absorption spectra.

Magenta couplers of the pyrazoloazole type, which are likewise preferred, may be represented by the formula ##STR33## in which R₁ is hydrogen or a substituent, Z represents the non-metallic atoms necessary to complete a 5-membered ring containing 2 or 3 nitrogen atoms, it being possible for this ring to be substituted, and Q is hydrogen or a leaving group.

Of these compounds, preference is given to magenta couplers of the formulae ##STR34## R₁₁, R₁₂ and R₃, independently of one another, are, for example, hydrogen, halogen, --CR₃ in which the radicals R, independently of one another, are hydrogen or alkyl, aryl, heterocyclyl, cyano, hydroxyl, nitro, carboxyl, amino, alkoxy, aryloxy, aeylamino, alkylamino, anilino, ureido, sulfamoylamino, alkylthio, arylthio, alkoxycarbonylamino, sulfonamido, carbamoyl, sulfamoyl, sulfonyl, alkoxycarbonyl, heterocyclyloxy, azo, acyloxy, carbamoyloxy, silyloxy, aryloxycarbonylamino, imido, heterocyclylthio, sulfinyl, phosphonyl, aryloxycarbonyl, acyl or azolyl, preferably hydrogen, halogen (for example chlorine or bromine), --CR₃ in which the radicals R₃, independently of one another, are hydrogen or alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, particularly preferably methyl, ethyl, propyl, isopropyl, t-butyl, tridecyl, 2-methanesulfonylethyl, 3-(3-pentadecylphenoxy)propyl, 3-(4-(2-(4-(4-hydroxyphenylsulfonyl)phenoxy)dodecanamido)phenyl)propyl, 2-ethoxytridecyl, trifluoromethyl, cyclopentyl, 3-(2,4-di-t-amylphenoxy)propyl; aryl (for example phenyl, 4-t-butylphenyl, 2,4-di-t-amylphenyl or 4-tetradecanamidophenyl); heterocyclyl (for example 2-furyl, 2-thienyl, 2-pyrimidinyl or 2-benzothiazolyl); cyano; hydroxyl, nitro; carboxyl; amino; alkoxy (for example methoxy, ethoxy, 2-methoxyethoxy; 2-dodecylethoxy, 2-methanesulfonylethoxy); aryloxy (for example phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, 3-t-butyloxycarbamoylphenoxy or 3-methoxycarbamoyl); acylamino (for example acetamido, benzamido, tetradecanamido, 2-(2,4-di-t-amylphenoxy)butanamido, 4-(3-t-butyl-4-hydroxyphenoxy)butanamido, 2-(4-(4-hydroxyphenylsulfonyl)phenoxy)decanamido or methylbutylamino); anilino (for example phenylamino, 2-chloroanilino, 2-chloro-5-tetradecanaminoanilino, 2-chloro-5-dodecyloxycarbonylanilino, N-acetylanilino, 2-chloro-5-(alpha-(3-t-butyl-4-hydroxyphenoxy)dodecanamidoanilino); ureido (for example phenylureido, methylureido or N,N-dibutylureido); sulfamoylamino (for example N,N-dipropylsulfamoylamino or N-methyl-N-decylsulfamoylamino); alkylthio (for example methylthio, octylthio, tetradecylthio, 2-phenoxyethylthio, 3-phenoxypropylthio or 3-(4-t-butylphenoxy)propylthio); arylthio (for example phenylthio, 2-butoxy-5-t-octylphenylthio, 3-pentadecylphenylthio, 2-carboxyphenylthio or 4-tetradecanamidophenylthio); alkoxycarbonylamino (for example methoxycarbonylamino or tetradecyloxycarbonylamino); sulfonamido (for example methanesulfonamido, hexadecanesulfonamido, benzenesulfonamido, p-toluenesulfonamido, octadecanesulfonamido or 2-methoxy-5-t-butylbenzenesulfonamido); carbamoyl (for example N-ethylcarbamoyl, N,N-di-butylcarbamoyl, N-(2-dodecyloxyethyl)carbamoyl, N-methyl-N-dodecylcarbamoyl or N-(3-(2,4-di-t-amylphenoxy)propyl)carbamoyl); sulfamoyl (for example N-ethyl-sulfamoyl, N,N-dipropylsulfamoyl, N-2-(dodecyloxyethyl)sulfamoyl, N-ethyl-N-dodecylsulfamoyl or N,N-diethylsulfamoyl); sulfonyl (for example methanesulfonyl, octanesulfonyl, benzenesulfonyl or toluenesulfonyl); alkoxycarbonyl (for example methoxycarbonyl, butoxycarbonyl, dodecyloxycarbonyl or octadecyloxycarbonyl); heterocyclyloxy (for example 1-phenyltetrazol-5-oxy or 2-tetrahydropyranyloxy); azo (for example phenylazo, 4-methoxyphenylazo, 4-pivaloylaminophenylazo or 2-hydroxy-4-propanoylphenylazo); acyloxy (for example acetoxy); carbamoyloxy (for example N-methylcarbamoyloxy or N-phenylcarbamoyloxy); silyloxy (for example trimethylsilyloxy or dibutylmethylsilyloxy); aryloxycarbonylamino (for example phenoxycarbonylamino); imido (for example N-succinimido, N-phthalimido or 3-octadecenylsuccinimido); heterocyclylthio (for example 2-benzothiazolylthio, 2,4-diphenyloxy-1,3,5-triazole-6-thio or 2-pyridylthio); sulfinyl (for example dodecanesulfinyl, 3-pentadecylphenylsulfinyl or 3-phenoxypropylsulfinyl); phosphonyl (for example phenoxyphosphonyl, octyloxyphosphonyl or phenylphosphonyl); aryloxycarbonyl (for example phenoxycarbonyl); acyl (for example acetyl, 3-phenylpropanoyl, benzoyl or 4-dodecyloxybenzoyl); or azolyl (for example imidazolyl, pyrazolyl or 3-chloropyrazol-1-yl).

These substituents may be further substituted, for example by halogen or by an organic radical bonded via a C, O, N or S atom.

Preferred groups R₁₁ are alkyl, aryl, alkoxy, aryloxy, alkylthio, ureido, urethane and acylamino groups.

R₁₂ may be as defined for R₁₁ and is preferably hydrogen, alkyl, aryl, a heterocyclic ring, alkoxycarbonyl, carbamoyl, sulfamoyl, sulfinyl, acyl or cyano.

R₁₃ may be as defined for R₁₁ and is preferably hydrogen, alkyl, aryl, a heterocyclic ring, alkoxy, aryloxy, alkylthio, arylthio, alkoxycarbonyl, carbamoyl or acyl, in particular alkyl, aryl, a heterocyclic ting, alkylthio or arylthio.

Q is hydrogen or a leaving group, such as halogen, alkoxy, aryloxy, acyloxy, alkyl- or arylsulfonyloxy, acylamino, alkyl- or arylsulfonamido, alkoxycarbonyloxy, aryloxycarbonyloxy, alkyl-, aryl- or heterocyclyl-S-carbamoylamino, a 5- or 6-membered, nitrogen-containing heterocyclic radical, imido or arylazo. These groups may be further substituted as indicated for R₁₁.

Q is preferably halogen (for example fluorine, chlorine or bromine); alkoxy (for example ethoxy, dodecyloxy, methoxyethylcarbamoylmethoxy, carboxypropoxy, methylsulfonylethoxy or ethoxycarbonylmethoxy); aryloxy (for example 4-methylphenoxy, 4-chlorophenoxy, 4-methoxyphenoxy, 4-carboxyphenoxy, 3-ethoxycarboxyphenoxy, 3-acetylaminophenoxy or 2-carboxyphenoxy); acyloxy (for example acetoxy, tetradecanoyloxy or benzoyloxy); alkyl- or arylsulfonyloxy (for example methanesulfonyloxy or toluenesulfonyloxy); acylamino (for example dichloroacetylamino or heptafluorobutyrylamino); alkyl- or arylsulfonamido (for example methanesulfonamido, trifluoromethanesulfonamido or p-toluenesulfonamido); alkoxycarbonyloxy (for example ethoxycarbonyloxy or benzyloxycarbonyloxy); aryloxycarbonyloxy (for example phenoxycarbonyloxy); alkyl-, aryl- or heterocyclyl-S- (for example dodecylthio, 1-carboxydodecylthio, phenylthio, 2-butoxy-5-t-octylphenylthio or tetrazolylthio); carbamoylamino (for example N-methylcarbamoylamino or N-phenylcarbamoylamino); a 5- or 6-membered, nitrogen-containing ring (for example imidazolyl, pyrazolyl, triazolyl, tetrazolyl or 1,2-dihydro-2-oxo-1-pyridyl); imido (for example succinimido or hydantoinyl); or arylazo (for example phenylazo or 4-methoxyphenylazo).

Q may alternatively form corresponding bis-compounds by condensation of 4 equivalents of coupler with an aldehyde or ketone. Furthermore, Q may contain photographically active groups, such as development inhibitors or development accelerators. Q is preferably halogen, alkoxy, aryloxy, alkyl- or arylthio, or a 5- or 6-membered, nitrogen-containing, heterocyclic group which is bonded to the coupling site via a nitrogen atom.

Pyrazolotetrazoles are described in JP-A 85/33 552; pyrazolopyrazoles in JP-A 85/43 695; pyrazoloimidazoles in JP-A 85/35 732, JP-A 86/18 949 and U.S. Pat. No. 4 500 630; pyrazolotriazoles in JP-A 85/186 567, JP-A 86/47 957, JP-A 85/215 687, JP-A 85/197 688, JP-A 85/172 982, EP-A 119 860, EP-A 173 256, EP-A 178 789, EP-A 178 788 and in Research Disclosure 84/24 624.

Further pyrazoloazole magenta couplers are described in: JP-A 86/28 947, JP-A 85/140 241, JP-A 85/262 160, JP-A 85/213 937, JP-A 87/278 552, JP-A 87/279 340, JP-A 88/100 457, EP-A 177 765, EP-A 176 804, EP-A 170 164, EP-A 164 130, EP-A 178 794, DE-A 3 516 996, DE-A 3 508 766 and Research Disclosure 81/20 919, 84/24 531 and 85/25 758.

Examples of suitable couplers of this type are: ##STR35##

Yellow couplers which can be used in the material according to the invention are preferably compounds of the formula A ##STR36## in which R₁ is alkyl or aryl, R₂ is aryl and Q is hydrogen or a group which can be eliminated by reaction with the oxidized developer.

A group of yellow couplers comprises the compounds of the formula A in which R₁ is t-butyl and R₂ is a group of the formula ##STR37## in which R₃ is hydrogen, halogen, alkyl or alkoxy, and R₄, R₅ and R₆ are hydrogen, halogen, alkyl, alkenyl, alkoxy, aryl, carboxyl, alkoxycarbonyl, carbamoyl, sulfonyl, sulfamoyl, alkylsulfonsulfonamamido, acylamino, ureido or amino.

Preferably, R₃ is chlorine, R₄ and R₅ are hydrogen and R₆ is an acylamino group. This group also includes the compounds of the formula ##STR38## in which x is 0-4, R₇ is hydrogen or alkyl, and R₈ and R₉ are alkyl.

Another group of yellow couplers conforms to the formula B ##STR39## in which R₁₀ is hydrogen, halogen or alkoxy, R₁₁, R₁₂ and R₁₃ are hydrogen, halogen, alkyl, alkenyl, alkoxy, aryl, carboxyl, alkoxycarbonyl, carbamoyl, sulfonyl, sulfamoyl, sulfonamido, acylamino, ureido or amino, and R₁ and Q are as defined above.

This group includes compounds of the formula B in which R₁ is t-butyl, R₁₀ is chlorine, R₁₁ and R₁₃ are hydrogen, and R₁₂ is alkoxycarbonyl.

In the compounds of the formulae A and B, leaving group Q may be hydrogen or a heterocyclic group ##STR40## in which R₁₄ is a divalent organic group which supplements the ring to make up a 4-7-membered ring, or Q is an --OR₁₅ group in which R₁₅ is alkyl, aryl, acyl or a heterocyclic radical.

Typical examples of customary yellow couplers are the compounds of the formulae below: ##STR41##

Further examples of yellow couplers are given in U.S. Pat. Nos. 2,407,210, 2,778,658, 2,875,057, 2 908,513, 2,908,573, 3,227,155, 3,227,550, 3,253,924, 3,265,506, 3,277,155, 3,408,194, 3,341,331, 3,369,895, 3,384,657, 3,415,652, 3,447,928, 3,551,155, 3,582,322, 3,725,072, 3,891,445, 3,933,501, 4,115,121, 4,401,752 and 4,022,620, in DE-A 1 547 868, 2,057,941, 2,162,899, 2,163,813, 2,213,461, 2,219,917, 2,261,361, 2,261,362, 2,263,875, 2,329,587, 2,414,006 and 2,422,812, in GB-A 1 425 020 and 1 077 874 and in JP-A 88/123 047 and in EP-A 447 969.

Typical and preferred yellow couplers conform to the formulae: ##STR42##

Cyan couplers may be, for example, derivatives of phenol, of 1-naphthol or of pyrazoloquinazolone. Preference is given to structures of the formula E ##STR43## in which R₂₁, R₂₂, R₂₃ and R₂₄ are hydrogen, halogen, alkyl, carbamoyl, amino, sulfonamido, phosphoramido or ureido. R₂₁ is preferably H or Cl, R₂₂ is preferably an alkyl or amino group, R₂₃ is preferably an amino group and R₂₄ is preferably hydrogen. Q" is hydrogen or a leaving group which is eliminated during the reaction with the oxidized developer. A detailed list of cyan couplers is given in U.S. Pat. No. 4,456,681.

Further examples of cyan couplers are given in the following: U.S. Pat. Nos. 2,369,929, 2,423,730, 2,434,272, 2,474,293, 2,521,293, 2,521,908, 2,698,794, 2,706,684, 2,772,162, 2,801,171, 2,895,826, 2,908,573, 3,034,892, 3,046,129, 3,227,550, 3,253,294, 3,311,476, 3,386,301, 3,419,390, 3,458,315, 3,476,560, 3,476,563, 3,516,831, 3,560,212, 3,582,322, 3,583,971, 3,591,383, 3,619,196, 3,632,347, 3,652,286, 3,737,326, 3,758,308, 3,839,044, 3,880,661, 4,004,929, 4,124,396, 4,333,999, 4,463,086, 4,456,681, 4,873,183 and 4,923,791 and in EP-A 354 549 and EP-A 398 664.

The red-sensitive silver-halide emulsion layer of the material according to the invention preferably contains a cyan coupler of the formula ##STR44## and/or of the formula ##STR45## in which Z₁ is alkyl or aryl, Z₂ is alkyl, cycloalkyl, aryl, a heterocyclic group or a ballast group, Z₃ is hydrogen or halogen, Z1 and Z₃ together can form a ring, and Z₄ is hydrogen or a leaving group, and Z₅ is a ballast group, Z₆ is hydrogen or a leaving group and Z₇ is alkyl.

Examples of customary cyan couplers are the following: ##STR46##

The colour developers usually used for colour-photographic materials are p-dialkylaminoanilines. Examples of these are 4-amino-N,N-diethylaniline, 3-methyl-4-amino-N,N-diethylaniline, 4-amino-N-ethyl-N-α-hydroxyethylaniline, 3-methyl-4-amino-N-ethyl-N-α-hydroxyethylaniline, 3-methyl-4-amino-N-ethyl-N-α-methanesulfonamidoethylaniline, 3-methyl-4-amino-N-ethyl-N-α-methoxyethylaniline, 3-α-methanesulfonamidoethyl-4-amino-N,N-diethylaniline, 3-methoxy-4-amino-N-ethyl-N-α-hydroxyethylaniline, 3methoxy-4-amino-N-ethyl-N-α-methoxyethylaniline, 3-acetamido-4-amino-N,N-diethylaniline, 4-amino-N,N-dimethylaniline, N-ethyl-N-α-[α'-(α"-methoxyethoxy)ethoxy]ethyl-3-methyl-4-aminoaniline, N-ethyl-N-α-(α'-methoxyethoxy)ethyl-3-methyl-4-aminoaniline, and the salts of these compounds, for example sulfates, hydrochlorides or toluenesulfonates.

The compounds of the formulae (I), (II), (III) and (IV) according to the invention, the magenta couplers and other colour couplers can be incorporated into the colour-photographic material in a known manner, for example into silver, halide emulsions which contain gelatin and/or other binders. They are used, for example, in silver-bromide, silver-chloride or silver-iodide emulsions or in emulsions which contain mixtures of silver halides, such as silver bromide/iodide or silver-chloride/bromide emulsions.

The compounds of the formulae (I), (II), (III) and (IV) according to the invention can be incorporated into the colour-photographic material together with the magenta coupler and if desired further additives by predissolving them in high-boiling organic solvents. Preference is given to solvents which boil higher than 160° C. Typical examples of these solvents are the esters of phthalic acid, phosphoric acid, citric acid, benzoic acid or fatty acids, and alkylamides and phenols.

A low-boiling solvent is usually used in addition in order to simplify incorporation of the additives into the colour-photographic material. Examples of such solvents are esters, for example ethyl acetate, alcohols, for example butanol, ketones, for example methyl isobutyl ketone, chlorinated hydrocarbons, for example methylene chloride, and amides, for example dimethylformamide. If the additives are themselves liquid, they can also be incorporated into the photographic material without the assistance of solvents.

The compounds according to the invention may if desired be dispersed in the gelatin layer as oil.

Further details on high-boiling solvents which can be used are given in the publications below:

Phosphates: GB-A 791 219, BE-A 755 248, JP-A 76/76 739, 78/27 449, 78/218 252, 78/97 573, 79/148 133, 82/216 177, 82/93 323 and 83/216 177 and EP-A 265 296.

Phthalates: GB-A 791 219, JP-A 77/98 050, 82/93 322, 82/216 176, 82/218 251, 83/24 321, 83/45 699 and 84/79 888.

Amides: GB-A 791 129, JP-A 76/105 043, 77/13 600, 77/61 089, 84/189 556, 87/239 149, EP-A 270 341 and WO 88/00 723.

Phenols: GB-A 820 329, FR-A 1 220 657, JP-A 69/69 946, 70/3 818, 75/123 026, 75/82 078, 78/17 914, 78/21 166, 82/212 114 and 83/45 699.

Other oxygen-containing compounds: U.S. Pat. Nos. 3,748,141, 3,779,765, JP-A 73/75 126, 74/101 114, 74/10 115, 75/101 625, 76/76 740, 77/61 089, EP-A 304 810 and BE-A 826 039.

Other compounds: JP-A 72/115 369, 72/130 258, 73/127 521, 73/76 592, 77/13 193, 77/36 294, 79/95 233, 91/2748, 193/105 147 and Research Disclosure 82/21 918.

The amount of high-boiling solvent is, for example, in the range from 50 mg to 2 g per m² of base, preferably from 200 mg to 1 g per m².

The photographic layers may furthermore contain colour cast inhibitors. These prevent colour casts being formed, due, for example, to reaction of the coupler with unintentionally oxidized developer or with by-products of the colour-formation process. Colour cast inhibitors of this type are usually hydroquinine derivatives, but may also be derivatives of aminophenols, of gallic acid or of ascorbic acid. Typical examples of these inhibitors are given in the publications below: U.S. Pat. Nos. 2,360,290, 2,336,327, 2,403,721, 2,418,613, 2,675,314, 2,701,197, 2,704,713, 2,728,659, 2,732,300, 2,735,365; EP-A 124 877, EP-A 277 589, EP-A 338 785; JP-A 75/92 988, 75/92 989, 75/93 928, 75/110 337, 84/5 247 and 77/146 235.

Photographic layers may also contain DIR couplers (DIR denotes Development Inhibition Release), which form colourless compounds with the oxidized developer. They are added to improve the sharpness and grain of the colour prints.

The photographic layers in the material according to the invention may also contain UV absorbers. These filter out the UV light and thus protect the dyes, the couplers and other components against photodegradation. Examples of such UV absorbers are 2-(2-hydroxyphenyl)benzotriazoles, 2-hydroxyphenyl-1,3,5-triazines, 2-hydroxybenzophenones, salicylic acid esters, acrylonitrile derivatives or thiazolines. UV absorbers of this type are described in greater detail, for example, in the following publications: U.S. Pat. Nos. 3,314,794, 3,352,681, 3,705,805, 3,707,375, 4,045,229, 3,700,455, 3,533,794, 3,698,907, 3,705,805, 3,738,837 and JP-A 71/2784. Preferred UV absorbers are the 2-(2-hydroxyphenyl)benzotriazoles (HBTs) of the formula ##STR47## in which T₁, T₂ and T₃, independently of one another, are hydrogen, halogen, alkyl, alkyl which is substituted by a carboxylate group, alkoxy, aryloxy, hydroxyl or acyloxy, and T₄ is hydrogen, alkoxy, aryloxy or acyloxy.

Particular preference is given to HBT compounds which are liquid at room temperature.

Examples of preferred HBT compounds are:

    ______________________________________                                          ##STR48##                                                                     HBT No. T.sub.1        T.sub.4        T.sub.3                                  ______________________________________                                         HBT-1   H              CH.sub.3       H                                        HBT-2   H              C(CH.sub.3).sub.3                                                                             H                                        HBT-3   C(CH.sub.3).sub.3                                                                             CH.sub.3       Cl                                       HBT-4   C(CH.sub.3).sub.3                                                                             C(CH.sub.3).sub.3                                                                             Cl                                       HBT-5   C(CH.sub.3).sub.2 C.sub.2 H.sub.5                                                             C(CH.sub.3).sub.2 C.sub.2 H.sub.5                                                             H                                        HBT-6   CH(CH.sub.3)C.sub.2 H.sub.5                                                                   C(CH.sub.3).sub.3                                                                             H                                        HBT-7                                                                                   ##STR49##                                                                                     ##STR50##     H                                        HBT-8   C(CH.sub.3).sub.3                                                                             CH.sub.2 CH.sub.2 COOC.sub.8 H.sub.17                                                         Cl                                                              (isomers)                                               HBT-9   C(CH.sub.3).sub.3                                                                             CH.sub.2 CH.sub.2 COOC.sub.8 H.sub.17                                                         H                                                               (isomers)                                               HBT-10  C.sub.12 H.sub.25 (isomers)*                                                                  CH.sub.3       H                                        ______________________________________                                          *Principal product                                                       

Other preferred UV absorbers are 2-hydroxyphenyl-1,3,5-triazines of the formula ##STR51## in which R₁ is a group of the formula ##STR52## where R₄, R₅ and R₆, independently of one another, are hydrogen, C₁ -C₁₂ alkyl or halogen, or R₁ is a group of the formula ##STR53## and R₂, R₃ and R₇, independently of one another, are monovalent organic radicals. R₂, R₃ and R₇ are preferably, independently of one another, a radical CH₂ CH(OR₈)CH₂ OR₉, where R₈ is hydrogen or acetyl, and R₉ is C₁ -C₄ alkyl ist.

The photographic layers may also contain phenolic Compounds which act as light stabilizers for the colour image and as colour cast inhibitors. They may be present in a light-sensitive layer (colour layer) or in an intermediate layer, alone or together with other additives. Such compounds are described in greater detail, for example, in the publications below: U.S. Pat. Nos. 3,700,455, 3,591,381, 3,573,052, 4,030,931, 4,174,220, 4,178,184, 4,228,235, 4,279,990, 4,346,165, 4,366,226, 4,447,523, 4,528,264, 4,581,326, 4,562,146, 4,559,297, GB-A 1 309 277, 1 547 302, 2 023 862, 2 135 788, 2 139 370, 2 156 091; DE-A 2 301 060, 2 347 708, 2 526 468, 2 621 203, 3 323 448; DD-A 200 691,214 468; EP-A 106 799, 113 124, 125 522, 159 912, 161 577, 164 030, 167 762, 176 845, 246 766, 320,776; JP-A 74/134 326, 76/127 730, 76/30 462, 77/3 822, 77/154 632, 78/10 842, 79/48 535, 79/70 830, 79/73 032, 79/147 038, 79/154 325, 79/155 836, 82/142 638, 83/224 353, 84/5246, 84/72 443, 84/87 456, 84/192 246, 84/192 247, 84/204 039, 84/204 040, 84/212 837, 84/220 733, 84/222 836, 84/228 249, 86/2540, 86/8843, 86/18 835, 86/18 836, 87/11 456, 87/42 245, 87/62 157, 86/6652, 89/137 258 and in Research Disclosure 79/17 804.

The photographic layers may also contain certain phosphorus(III) compounds, in particular phosphites and phosphonites. These act as light stabilizers for the colour images and as dark-storage stabilizers for magenta couplers. They are preferably added to the high-boiling solvents together with the coupler. Phosphorus(III) compounds of this type are described in greater detail, for example, in the publications below: U.S. Pat. No. 4,407,935, U.S. Pat. No. 4,436,811, U.S. Pat. No. 4,956,406, EP-A 181 289, JP-A 73/32 728, JP-A 76/1420 and JP-A 55/66 741.

The photographic layers may also contain organometallic complexes which are light stabilizers for the colour images, in particular for the magenta dyes. Such compounds and combinations thereof with other additives are described in greater detail, for example, in the publications below: U.S. Pat. Nos. 4,050,938, 4,239,843, 4,241,154, 4,242,429, 4,241,155, 4,242,430, 4,273,854, 4,246,329, 4,271,253, 4,242,431, 4,248,949, 4,245,195, 4,268,605, 4,246,330, 4,269,926, 4,245,018, 4,301,223, 4,343,886, 4,346,165, 4,590,153; JP-A 81/167 138, 81/168 652, 82/30 834, 82/161 744; EP-A 137 271, 161 577, 185 506; DE-A 2 853 865.

The photographic layers may also contain hydroquinone compounds. These act as light stabilizers for the colour couplers and for the colour images and as scavengers of oxidized developer in the intermediate layers. They are used in particular in the magenta layer. Hydroquinone compounds of this type and combinations thereof with other additives are described in greater detail, for example, in the publications below: U.S. Pat. Nos. 2,360,290, 2,336,327, 2,403,721, 2,418,613, 2,675,314, 2,701,197, 2,710,801, 2,732,300, 2,728,659, 2,735,765, 2,704,713, 2,937,086, 2,816,028, 3,582,333, 3,637,393, 3,700,453, 3,960,570, 3,935,016, 3,930,866, 4,065,435, 3,982,944, 4,232,114, 4,121,939, 4,175,968, 4,179,293, 3,591,381, 3,573,052, 4,279,990, 4,429,031, 4,346,165, 4,360,589, 4,346,167, 4,385,111, 4,416,978, 4,430,425, 4,277,558, 4,489,155, 4,504,572, 4,559,297, FR-A 885 982; GB-A 891 158, 1 156 167, 1 363 921, 2 022 274, 2 066 975, 2 071 348, 2 081 463, 2 117 526, 2 156 091; DE-A 2 408 168, 2 726 283, 2 639 930, 2 901 520, 3 308 766, 3 320 483, 3 323 699; DD-A 216 476,214 468, 214 469, EP-A 84 290, 110 214, 115 305, 124 915, 124 877, 144 288, 147 747, 178 165, 161 577; JP-A 75/33 733, 75/21 249, 77/128 130, 77/146 234, 79/70 036, 79/133 131, 81/83 742, 81/87 040, 81/109 345, 83/134 628, 82/22 237, 82/112 749, 83/17 431, 83/21 249, 84/75 249, 84/149 348, 84/182 785, 84/180 557, 84/189 342, 84/228 249, 84/101 650, 79/24 019, 79/25 823, 86/48 856, 86/48 857, 86/27 539, 86/6652, 86/72 040, 87/11 455, 87/62 157, and in Research Disclosure 79/17 901, 79/17 905, 79/18 813, 83/22 827 and 84/24 014.

The photographic layers may also contain further derivatives of hydroquinone ethers. These compounds act as light stabilizers and are particularly suitable for stabilising magenta dyes. Such compounds and combinations thereof with other additives are described in greater detail, for example, in the publications below: U.S. Pat. No. 3,285,937, 3,432,300, 3,519,429, 3,476,772, 3,591,381, 3,573,052, 3,574,627, 3,573,050, 3,698,909, 3,764,337, 3,930,866, 4,113,488, 4,015,990, 4,113,495, 4,120,723, 4,155,765, 4,159,910, 4,178,184, 4,138,259, 4,174,220, 4,148,656, 4,207,111, 4,254,216, 4,134,011, 4,273,864, 4,264,720, 4,279,990, 4,332,886, 4,436,165, 4,360,589, 4,416,978, 4,385,111, 4,459,015, 4,559,297, 4,631,252, 4,616,082; GB-A 1 347 556, 1 366 441, 1 547 392, 1 557 237, 2 135 788; DE-A 3 214 567, 4 008 785, 4 012 305; DD-214 469, EP-A 161 577, 167 762, 164 130, 176 845; JP-A 76/123 642, 77/35 633, 77/147 433, 78/126, 78/10 430, 78/53 321, 79/24 019, 79/25 823, 79/48 537, 79/44 521, 79/56 833, 79/70 036, 79/70 830, 79/73 032, 79/95 233, 79/145 530, 80/21 004, 80/50 244, 80/52 057, 80/70 840, 80/139 383, 81/30 125, 81/151 936, 82/34 552, 82/68 833, 82/204 306,.82/204 037, 83/134 634, 83/207 039, 84/60 434, 84/101 650, 84/87 450, 84/149 348, 84/182 785, 86/72 040, 87/11 455, 87/62 157, 87/63 149, 86/2151, 86/6652, 86/48 855, 89/309 058 and in Research Disclosure 78/17 05 1.

Preferred co-stabilizers conform to the following formulae P, SA, SB, HQ, RE, KA and KB.

Compounds of formula P ##STR54## where R₁ and R₂, independently of one another, are hydrogen, acyl or alkyl;

R_(a), R_(b) and R_(c), independently of one another, are H, alkyl, cycloalkyl, aryl, halogen, alkoxy, aroxy, acyloxy, alkylthio, arylthio, acyl, ;sulphonyl, sulphamoyl, acylamino, sulphonylamino or nitro;

A is a bond, S═[O]_(m), alkylene or NR_(d) ;

R_(d) is alkyl or acyl; and

m is 0, 1 or 2.

Examples of compounds of formula P: ##STR55##

Compounds of formula SA ##STR56## where R₁ is hydrogen;

R₂ is phenyl or

R₁ and R₂ are methyl;

q is 0, 1 or 2; and

X is a divalent radical, which completes the ring in formula SA to give a tetrahydrothiopyrane.

Examples of compounds of formula SA (see also U.S. Pat. No. 4,993,271): ##STR57##

Compounds of formula SB

R₃ --S--(C_(p) H_(2p))--Z--R₄

where

R₃ is alkyl, aryl or a group (C_(p) H_(2p))--Z--R₄ ;

p is 1-12;

Z is --CO--O-- or --O--CO--;

R₄ is a mono-, di-, tri- or tetra-valent group.

Examples of compounds of the formula SB ##STR58##

Compounds of the formula HQ ##STR59## where R_(e) and R_(d), independently of one another, are alkyl or cycloalkyl; and

R_(f) and R_(g), independently of one another, are as R_(a), R_(b) and R_(c).

Examples of compound of the formula HQ ##STR60##

Compounds of the formula RE ##STR61## where R₁ and R_(m), independently of one another, are H, acyl or alkyl; or R_(l) and R_(m) are bound together to a P--O-aryl radical; and

R_(h), R_(i), R_(j) and R_(k), independently of one another, are as R_(a), R_(b) and R_(e), provided that at least one of the radicals R_(i) or R_(j) is not alkyl.

Examples of compounds of the formula RE ##STR62##

Compounds of formula KA ##STR63## where R_(n) is alkyl, cycloalkyl or aryl;

p is 0, 1 or 2; and

R_(o), R_(p), R_(q) and R_(r), independently of one another, are as R_(a), R_(b) and R_(c).

Examples of compounds of the formula KA ##STR64##

Compounds of formula KB ##STR65## where, X is a bond, ##STR66## R_(t) is alkyl, aryl, acyl or sulphonyl; and R_(s) is as R_(a), R_(b) and R_(c).

Examples of compounds of the formula KB ##STR67##

Silver-halide emulsions which can be used are conventional silver-chloride, silver-bromide or silver-iodide emulsions or mixtures thereof, such as silver-chlorobromide and silver-chloroiodide emulsions, in which the silver halides may have any known crystal form. The use of silver-chloride emulsions is particularly important in the material according to the invention. The preparation of such emulsions and the sensitization thereof are described in RESEARCH DISCLOSURE, November 1989, No. 307 105. This publication furthermore mentions a number of binders for said emulsions which can also be used in the materials according to the invention. The same applies to the bases mentioned in the publication.

The silver-halide emulsion which can be used for carrying out this invention can be sensitized for all desired wavelengths with the aid of sensitization pigments. For this purpose, it is possible to use cyanine pigments, merocyanine pigments, holopolar pigments, hemicyanine pigments, styryl pigments or hemioxanol pigments.

The photographic layers may furthermore contain conventional plasticizers, such as glycerol. The emulsions may also be cured by means of curing agents which are customary for gelatin. Finally, the emulsions may also contain customary coating auxiliaries.

The present invention thus furthermore relates to colour-photographic recording materials according to claim 1, which contain further organic stabilizers, UV absorbers, optical brighteners, light stabilizers, colour cast inhibitors and/or plasticizers.

The present invention also relates to compounds of the formula ##STR68## in which R₁ and R₃, independently of one another, are hydrogen, C₁ -C₁₂ alkyl, C₅ -C₇ cycloalkyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl groups, phenyl-C₁ -C₄ alkyl, phenyl, C₁ -C₄ alkoxy or a group of the formula V ##STR69## in which R₈ and R₉, independently of one another, are C₁ -C₈ alkyl,

n is 1-10, and

R₁₀ is hydrogen, C₁ -C₂₄ alkyl, which is unsubstituted or interrupted by one or more O atoms and is unsubstituted or substituted by one --OH, or is C₂ -C₁₈ alkenyl, C₅ -C₁₂ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₄ alkyl, or is phenyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl, or is phenyl-C₁ -C₄ alkyl or furfuryl;

R₂ and R₄, independently of one another, are hydrogen or C₁ -C₄ alkyl;

R₅ is hydrogen, --CO--R₁₁, --CO--OR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₁₈ alkyl or phenyl, R₁₂ is C₁ -C₄ alkyl, and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl or phenyl; R₇ is hydrogen, C₁ -C₁₂ alkyl, which is uninterrupted or interrupted by one or more --O--, --S-- or --SO₂ --, or is C₅ -C₁₂ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₄ alkyl, or is phenyl-C₁ -C₄ alkyl, a group of the formula VI ##STR70## or a group of the formula VIIa

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 OR.sub.16                  VIIa,

in which R₅ and R₁₆ are as defined for formula (Ia),

R₁₇ is hydrogen or C₁ -C₁₈ alkyl, and

R₁₈ is C₁ -C₁₂ alkyl, which is unsubstituted or interrupted by one or more O atoms, or is C₂ -C₁₈ alkenyl, benzyl or phenyl, which is unsubstituted or substituted by 1-3

C₁ -C₄ alkyl; and

the radicals R₁₆, independently of one another, are hydrogen, C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl, phenyl-C₁ -C₄ alkyl, C₃ -C₂₄ alkyl or C₂ -C₁₄ hydroxyalkyl, each of which is interrupted by one or more O atoms, or are phenyl, tolyl, C₅ -C₆ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₈ alkyl, or --CO--R₁₁, in which

R₁₁ is C₁ -C₁₈ alkyl or phenyl.

Preferred compounds are those of the formula ##STR71## in which R₁ and R₃, independently of one another, are hydrogen, C₁ -C₁₂ alkyl, C₅ -C₆ cycloalkyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl groups, phenyl-C₁ -C₄ alkyl, phenyl, C₁ -C₈ alkoxy or a group of the formula V ##STR72## in which R₈ and R₉, independently of one another, are C₁ -C₈ alkyl;

n is 1-10, and

R₁₀ is hydrogen, C₁ -C₂₄ alkyl, which is unsubstituted or interrupted by one or more O atoms and unsubstituted or substituted by one --OH, or is C₂ -C₁₈ alkenyl, C₅ -C₁₂ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₄ alkyl, or is phenyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl, or is phenyl-C₁ -C₄ alkyl or furfuryl;

R₂ and R₄, independently of one another, are hydrogen or C₁ -C₁₂ alkyl;

R₅ is hydrogen, --CO--R₁₁, --CO--OR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₁₂ alkyl, R₁₂ is C₁ -C₄ alkyl, and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl or phenyl; and the radicals R₁₆, independently of one another, are C₁ -C₁₈ alkyl, C₂ -C₁₀ alkenyl, benzyl, C₃ -C₁₈ alkyl which is interrupted by one or more O atoms, cyclohexyl or --CO--R₁₁, in which

R₁₁ is C₁ -C₁₂ alkyl.

Particular preference is given to compounds of the formula ##STR73## in which R₁ and R₃, independently of one another, are hydrogen, C₁ -C₁₂ alkyl, C₅ -C₆ cycloalkyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl groups, phenyl-C₁ -C₄ alkyl, phenyl, C₁ -C₈ alkoxy or a group of the formula V ##STR74## in which R₈ and R₉, independently of one another, are C₁ -C₈ alkyl;

n is 1-10, and

R₁₀ is hydrogen, C₁ -C₂₄ alkyl, which is unsubstituted or interrupted by one or more O atoms and is unsubstituted or substituted by one --OH, or is C₂ -C₁₈ alkenyl, C₅ -C₁₂ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₄ alkyl, or is phenyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl, or is phenyl-C₁ -C₄ alkyl or furfuryl;

R₂ and R₄, independently of one another, are hydrogen or C₁ -C₁₂ alkyl;

R₅ is hydrogen, --CO--R₁₁, --CO--OR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₄ alkyl, R₁₂ is C₁ -C₄ alkyl, and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl or phenyl; and the radicals R₁₆, independently of one another, are C₁ -C₁₈ alkyl, allyl, benzyl, C₃ -C₁₂ alkyl which is interrupted by one or more O atoms, cyclohexyl or --CO--R₁₁, in which

R₁₁ is C₁ -C₄ alkyl.

Very particularly preference is given to compounds of the formula ##STR75## in which R₁, R₃ and R₄, independently of one another, are hydrogen or C₁ -C₈ alkyl;

R₂ is hydrogen;

R₅ is hydrogen or --CO--CH₃ ; and the radicals R₁₆, independently of one another, are C₁ -C₁₂ alkyl, allyl or C₃ -C₇ alkyl which is interrupted by 1-3 O atoms.

The present invention furthermore relates to compounds of the formulae III ##STR76## and IV ##STR77## in which R₁, R₂, R₃, R₄, R₅, R₆, R₁₉, A₁, A₂ and m are as defined in claim 1.

Further preferred compounds are those mentioned in the description of the photographic material.

The compounds according to the invention can be prepared by methods known per se, for example by reacting a compound of one of the formulae ##STR78## with a glycidyl ether of the formula ##STR79## in which the radicals R₁, R₂, R₃, R₄ and R₁₆ are as defined in claim 1. ##STR80##

Compounds according to the invention in which R₅ is not hydrogen can be prepared by further reacting with an acylating agent or silylating agent, for example ##STR81##

The polymeric compounds of the formula (IV) can be prepared by reacting a compound of the formula (I°) with a bisglycidyl ether of the formula

The examples below illustrate the invention in greater detail.

EXAMPLE 1

Preparation of 1,4-di(3'-butoxy-2'-hydroxypropoxy)-2,5-dimethylbenzene 20 g of 2,5-dimethylhydroquinone, 42.2 g of butyl glycidyl ether and 5.3 g of ethyltriphenylphosphonium bromide are stirred for 15 hours in 80 ml of boiling xylene. The mixture is then allowed to cool to room temperature, the organic phase is washed with water and dried, and the solvent is evaporated. The crude product is chromatographed on silica gel, giving 27.5 g of 1,4-di(3'-butoxy-2'-hydroxypropoxy)-2,5-dimethylbenzene as a yellowish oil (m.p. <30° C.).

Elemental analysis: C₂₂ H₃₈ O₆ Calculated: C 66.30; H 9.61% Found: C 66.00; H 9.70 %

EXAMPLE 2

If Example 1 is repeated, but with the 2,5-dimethylhydroquinone replaced by the corresponding amount of 2,5-di-tert-butylhydroquinone, 28.7 g of 1,4-di(3'-butoxy-2'-hydroxypropoxy)-2,5-di-tert-butylbenzene are obtained as a white solid (m.p. 59° C.)

Elemental analysis: C₂₈ H₅₀ O₆ Calculated: C 69.67; H 10.44 % Found: C 69.31; H 10.41%

EXAMPLES 1a and 2a

A procedure analagous to Examples 1 and 2 gives the compounds 1-48 mentioned above, which have a melting point of <20° C., with the exception of Compounds 1 (59°-60° C.), 2 (76° C.), 12 (40°-41° C.), 13 (58°-60°), 26 (131° C.), 30 (116°-123° C.) and 37 (31°-32° C.).

EXAMPLE 3

A polyethylene-coated support material is coated with a gelatin layer containing silver bromide, magenta coupler (M-6) and a stabilizer.

The gelatin layer contains the following components (per m² of support material):

                  TABLE 1                                                          ______________________________________                                         Component        Ag Br layer                                                   ______________________________________                                         Gelatin          5.15         g                                                Curing agent     300          mg                                               Wetting agent    85           mg                                               Silver bromide   260          mg                                               Magenta coupler  325          mg                                               Tricresyl phosphate                                                                             162          mg                                               Stabilizer       114          mg                                               ______________________________________                                    

The curing agent used is 2,4-dichloro-6-hydroxytriazine, and the wetting agent used is the sodium salt of diisobutylnapthalenesulfonic acid.

A step wedge having a density difference of 0.15 logE per step is exposed onto each of the resultant samples, which are subsequently processed in accordance with the manufacturer's instructions by the Kodak EP2 process for colour negative papers.

After exposure and processing, the remission density in green for the magenta step is measured at a density between 0.9 and 1.1 of the wedge. The wedge is then exposed behind a UV absorber filter in an Atlas exposure unit with 15 kJ/cm², and the remission density is re-measured. The drop in magenta dye density (-ΔD) is shown in Table 2 in %.

                  TABLE 2                                                          ______________________________________                                         Sample No.      Stabilizer                                                                              -ΔD                                             ______________________________________                                         1               none     87                                                    2               3        53                                                    3               14       54                                                    ______________________________________                                    

EXAMPLE 4

The procedure is as in Example 3, but the Kodak RA4 process is used. The drop in magenta dye density (-ΔD) is shown in Table 3 in %.

                  TABLE 3                                                          ______________________________________                                         Sample No.      Stabilizer                                                                              -ΔD                                             ______________________________________                                         4               none     81                                                    5               14       44                                                    ______________________________________                                    

It can be seen from Examples 3 and 4 that the novel compounds are good light stabilizers.

EXAMPLE 5

The procedure is as in Example 3, but the stabilizer is used as an oil. The amounts of oil are shown in Table 4. A second step wedge is measured in blue in order to determine the yellowing. The wedge is then stored for 28 days in a conditioning cabinet at 75° C. and 60 % relative humidity, the remission density (in blue) is re-measured, and the increase in yellow dye density (-ΔD_(B)) is calculated.

The drop in magenta dye density (-ΔD) in % and the yellowing (-ΔD_(B)) are shown in Table 4. The drop in dye density (-ΔD) is also shown for a magenta dye density of 2 in Table 4.

                  TABLE 4                                                          ______________________________________                                         Sample              Amount   -ΔD (%)                                     No    Oil           (mg/m.sup.2)                                                                            D = 1 D = 2 -ΔD.sub.B                       ______________________________________                                         6     Tricresyl phosphate                                                                          276      84    81    0.12                                  7     Tricresyl phosphate                                                                          325      82    78    0.11                                  8     Tricresyl phosphate                                                                          440      79    71    0.11                                  9     14            276      60    57    0.11                                  10    14            325      45    33    0.12                                  11    14            440      40    22    0.12                                  ______________________________________                                    

It can be seen that the drops in dye density for D=1 and D=2 are much lower than for the conventional oil tricresyl phosphate. Climatic yellowing of the stabilizer (oil) of the invention is, within the limit of experimental accuracy, the same as that for the conventional oil (tricresyl phosphate).

EXAMPLE 6

The procedure is as in Example 5, but 306 mg of the magenta coupler (M-5) are used. The Atlas yellowing is also measured; to this end, the remission density in blue is measured in order to determine the yellowing. The wedge is then exposed in an Atlas exposure unit with 30 kJ/cm², the remission density (in blue) is re-measured, and the increase in yellow dye density (-ΔD_(B)) is calculated. The drop in magenta dye density (-ΔD) after 30 kJ/cm² exposure and the yellowing (-ΔD_(B)) are shown in Table 5.

                  TABLE 5                                                          ______________________________________                                         Sample               Amount                                                    No.   Oil            (mg/m.sup.2)                                                                             -ΔD                                                                             -ΔD.sub.B                          ______________________________________                                         12    Tricresyl phosphate                                                                           612       42     0.02                                     13    14             612       8      0.00                                     14    14             918       7      0.00                                     ______________________________________                                    

It can be seen that, here too, the novel compounds are very highly suitable as a photographic oil having light stabilization properties for magenta couplers/dyes.

EXAMPLE 7

The procedure is as in Example 3, but the novel compounds are used as oils (325 mg/m²) for further light stabilizers. The further light stabilizer used conforms to the formula: ##STR83## and is employed in an amount of 114 mg/m². The drop in magenta dye density (-ΔD) and the climatic yellowing (-ΔD_(B)) are shown in Table 6.

                  TABLE 6                                                          ______________________________________                                         Sample                                                                         No.   Oil            Stabilizer                                                                               -ΔD                                                                             -ΔD.sub.B                          ______________________________________                                         15    Tricresyl phosphate                                                                           --        82     0.11                                     16    Tricresyl phosphate                                                                           L-1       50     0.19                                     17    14             --        45     0.12                                     18    14             L-1       38     0.18                                     ______________________________________                                    

It can be seen that the novel compounds not only act as light stabilizers, but are also suitable as coupler solvents (oils).

EXAMPLE 8

The procedure is as in Example 3, but the Kodak RA4 process is used, magenta coupler M-11 (204 mg) is used, the stabilizer is employed in an amount of 102 mg, and a 30 kJ/cm.sup. 2 exposure is carried out. The drop in magenta dye density is shown in Table 7 in %.

                  TABLE 7                                                          ______________________________________                                         Sample                                                                         No.           Stabilizer                                                                              -ΔD (%)                                           ______________________________________                                         19            none     91                                                      20            16       56                                                      21            32/k     59                                                      ______________________________________                                    

EXAMPLE 9

The procedure is as in Example 8, but the stabilizer is used as an oil (408 mg,/m²), and no tricresyl phosphate is employed in samples 23-25. The drop in magenta dye density is shown in Table 8 in %.

                  TABLE 8                                                          ______________________________________                                         Sample                                                                         No.         Oil           -ΔD (%)                                        ______________________________________                                         22          Tricresyl phosphate                                                                          92                                                   23          16            36                                                   24          14            34                                                   25          32/j          34                                                   ______________________________________                                    

EXAMPLE 10

The procedure is as in Example 9, but the amount of oil is 204 mg/m², and no tricresyl phosphate is employed in samples 27 and 28. The drop in magenta dye density is shown in Table 9 in %.

                  TABLE 9                                                          ______________________________________                                         Sample                                                                         No.         Oil           -ΔD (%)                                        ______________________________________                                         26          Tricresyl phosphate                                                                          91                                                   27          14            40                                                   28          32/c          32                                                   ______________________________________                                    

EXAMPLE 11

The procedure is as in Example 10, but the novel compounds are used as an oil (204 mg/m²) for further stabilizers. The further stabilizers used conform to the formulae ##STR84## and are employed in an amount of 102 mg/m², and no tricresyl phosphate is employed in samples 33-39. The drop in magenta dye density is shown in Table 10 in %.

                  TABLE 10                                                         ______________________________________                                         Sample                                                                         No.     Oil             Stabilizer                                                                              -ΔD (%)                                 ______________________________________                                         29      Tricresyl phosphate                                                                            --       91                                            30      Tricresyl phosphate                                                                            P 1      55                                            31      Tricresyl phosphate                                                                            P 2      70                                            32      Tricresyl phosphate                                                                            SA 1     88                                            33      14              --       40                                            34      14              P 1      24                                            35      14              P 2      30                                            36      14              SA 1     28                                            37      32/c            --       32                                            38      32/c            P 1      22                                            39      32/c            SA 1     23                                            ______________________________________                                     

What is claimed is:
 1. A colour-photographic recording material which contains a magenta coupler and, as stabilizer, at least one compound of the formula ##STR85## where R₁ and R₃, independently of one another, are hydrogen, C₁ -C₁₂ alkyl, C₅ -C₇ cycloalkyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl groups, phenyl-C₁ -C₄ alkyl, phenyl, C₁ -C₄ alkoxy or a group of the formula V ##STR86## in which R₈ and R₉, independently of one another, are C₁ -C₈ alkyl,n is 1-10, and R₁₀ is hydrogen, C₁ -C₂₄ alkyl, which is unsubstituted or interrupted by one or more O atoms and is unsubstituted or substituted by one --OH group, or is C₂ -C₁₈ alkenyl, C₅ -C₁₂ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₄ alkyl, or is phenyl, which is unsubstituted or substituted by one or two C₁ -C₄ alkyl, or is phenyl-C₁ -C₄ alkyl or furfuryl; R₂ and R₄, independently of one another, are hydrogen or C₁ -C₁₂ alkyl; R₅ is hydrogen, --CO--R₁₁, --CO--OR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl, R₁₂ is C₁ -C₄ alkyl and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl or phenyl; the radicals R₆, independently of one another, are --OR₁₆ or C₁ -C₁₅ alkyl, in which R₁₆ is hydrogen, C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl, phenyl-C₁ -C₄ alkyl, C₃ -C₂₄ alkyl or C₂ -C₁₄ hydroxyalkyl, each of which is interrupted by one or more O atoms, or is phenyl, which is unsubstituted or substituted by C₁ -C₄ alkyl, C₁ -C₄ alkoxy or halogen, tolyl, C₅ -C₆ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₈ alkyl, or is --CO--R₁₁, in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl; R₇ is a group of the formula VI ##STR87## or a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ and R₆ are as defined for formula I, R₁₇ is hydrogen or C₁ -C₁₈ alkyl, and R₁₈ is C₁ -C₁₂ alkyl, which is unsubstituted or interrupted by one or more O atoms, or is C₂ -C₁₈ alkenyl, benzyl or phenyl, which is unsubstituted or substituted by 1-3 C₁ -C₄ alkyl; R₁₉ is C₂ -C₁₀ alkylene, phenylene or a -phenylene-R₂₀ -phenylene- group, in which R₂₀ is --O--, --S--, --SO₂ --, --CH₂ -- or --C(CH₃)₂ --; m is 1-100; A₁ is hydrogen, --CH₂ CH(OR₅)CH₂ OR₁₉ OCH(OR₅)CH₂ OR₅ or ##STR88## and A₂ is --OH or ##STR89## or R₃ and R₇ in the formula I, together with the atoms to which they are bonded, form a C₅ -C₆ ring, which is unsubstituted or substituted by 1 to 3 C₁ -C₈ alkyl.
 2. A colour-photographic recording material according to claim 1, which contains, as stabilizer, at least one compound of the formula ##STR90## in which R₁ and R₃, independently of one another, are hydrogen, C₁ -C₈ alkyl, cyclohexyl, --C(CH₃)₂ C₆ H₅, C₁ -C₄ alkoxy or a group of the formula V ##STR91## in which R₅ and R₉ are methyl; n is 3, andR₁₀ is hydrogen, C₁ -C₁₂ alkyl, which is unsubstituted or interrupted by one or more O atoms and is unsubstituted or substituted by one --OH, or is C₂ -C₁₈ alkenyl or benzyl; R₂ is hydrogen; R₄ is hydrogen or C₁ -C₈ alkyl; R₅ is hydrogen, --CO--R₁₁, --CO--OR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl, R₁₂ is C₁ -C₄ alkyl, and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl or phenyl; the radicals R₆ independently of one another, are --OR₁₆, in which R₁₆ is hydrogen, C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl, phenyl-C₁ -C₄ alkyl, C₃ -C₂₄ alkyl or C₂ -C₁₄ hydroxyalkyl, each of which is interrupted by one or more O atoms, or is phenyl, tolyl, C₅ -C₆ cycloalkyl, which is unsubstituted or substituted by 1 to 3 C₁ -C₈ alkyl, or is --CO--R₁₁, in which R₁₁ is C₁ -C₁₈ alkyl, C₂ -C₁₈ alkenyl or phenyl; R₇ is a group of the formula VI ##STR92## or a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ and R₆ are as defined for formula I, R₁₇ is hydrogen or C₁ -C₁₂ alkyl, and R₁₈ is C₁ -C₈ alkyl; R₁₉ is C₂ -C₈ alkylene, phenylene or a -phenylene-R₂₀ -phenylene- group, in which R₂₀ is --SO₂ --, --CH₂ -- or --C(CH₃)₂ --; m is 1-50; A₁ is hydrogen, --CH₂ CH(OR₅)CH₂ OR₁₉ OCH(OR₅)CH₂ OR₅ or ##STR93## and A₂ is --OH or ##STR94##
 3. A colour-photographic recording material according to claim 1, which contains, as stabilizer, at least one compound of the formula ##STR95## in which R₁ and R₃, independently of one another, are hydrogen, C₁ -C₈ alkyl, C₁ -C₄ alkoxy or a group of the formula V ##STR96## in which R₈ and R₉ are methyl, n is 3, andR₁₀ is C₁ -C₄ alkyl; R₂ is hydrogen; R₄ is hydrogen or C₁ -C₈ alkyl; R₅ is hydrogen, CO--R₁₁, --COOR₁₂ or --Si(R₁₃)(R₁₄)(R₁₅), in which R₁₁ is C₁ -C₄ alkyl or C₂ -C₃ alkenyl, R₁₂ is C₁ -C₄ alkyl, and R₁₃, R₁₄ and R₁₅, independently of one another, are C₁ -C₆ alkyl; the radicals R₆, independently of one another, are --OR₁₆, in which R₁₆ is C₁ -C₁₈ alkyl, allyl, benzyl, phenyl, C₃ -C₁₂ alkyl which is interrupted by one or more O atoms, or is cyclohexyl or --CO--R₁₁, in which R₁₁ is C₁ -C₄ alkyl or C₂ -C₃ alkenyl; R₇ is a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ and R₆ are as defined for formula I; R₁₉ is C₂ -C₈ alkylene or a phenylene-R₂₀ -phenylene- group, in which R₂₀ is --C(CH₃)₂ --; m is 1-25; A₁ is hydrogen, --CH₂ CH(OR₅)CH₂ OR₁₉ OCH(OR₅)CH₂ OR₅ or ##STR97## and A₂ is --OH or ##STR98##
 4. A colour-photographic recording material according to claim 1, which contains, as stabilizer, at least one compound of the formula ##STR99## in which R₁, R₃ and R₄, independently of one another, are hydrogen or C₁ -C₈ alkyl;R₂ is hydrogen; R₅ is hydrogen or --CO--CH₃ ; R₁₆ is C₁ -C₁₂ alkyl, allyl or C₃ -C₇ alkyl which is interrupted by 1-3 O atoms; and R₇ is a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ is as defined for formula I and R₆ is --OR₁₆.
 5. A colour-photographic recording material according to claim 1, which contains, as stabilizer, at least one compound of the formula ##STR100## in which R₁, R₃ and R₄, independently of one another, are hydrogen or C₁ -C₈ alkyl;R₂ is hydrogen; R₅ is hydrogen; R₁₆ is C₁ -C₁₂ alkyl, and R₇ is a group of the formula VII

    --CH.sub.2 CH(OR.sub.5)CH.sub.2 R.sub.6                    VII,

in which R₅ is as defined for formula I and R₆ is --OR₁₆.
 6. A colour-photographic recording material according to claim 1, which contains further organic stabilizers, UV absorbers, optical brighteners, light stabilizers, colour east inhibitors and/or plasticizers.
 7. A colour-photographic recording material according to claim 1, which contains at least one further organic stabilizer of one of the following formulae P, SA, SB, HQ, RE, KA or KB formula P ##STR101## where R₁ and R₂, independently of one another, are hydrogen, acyl or alkyl;R_(a), R_(b) and R_(c), independently of one another, are H, alkyl, cycloalkyl, aryl, halogen, alkoxy, aroxy, acyloxy, alkylthio, arylthio, acyl, sulphonyl, sulphamoyl, acylamino, sulphonylamino or nitro; A is a bond, S═O_(m), alkylene or NR_(d) ; R_(d) is alkyl or acyl; and m is 0, 1 or 2;formula SA ##STR102## where R₁ is hydrogen; R₂ is phenyl or R₁ and R₂ are methyl; q is 0, 1 or 2; and X is a divalent radical, which completes the ring in formula SA to give a tetrahydrothiopyrane;formula SB R₃ --S--(C_(p) H_(2p))--Z--R₄ where R₃ is alkyl, aryl or a group (C_(p) H_(2p))--Z--R₄ ; p is 1-12; Z is --CO--O-- or --O--CO--; R₄ is a mono-, di-, tri- or tetra-valent group;formula HQ ##STR103## where R_(e) and R_(d), independently of one another, are alkyl or cycloalkyl; and R_(f) and R_(g), independently of one another, are as R_(a), R_(b) and R_(c) ;formula RE ##STR104## where R_(l) and R_(m), independently of one another, are H, acyl or alkyl; or R_(l) and R_(m) are bound together to a P--O-aryl radical; and R_(h), R_(i), R_(j) and R_(k), independently of one another, are as R_(a), R_(b) and R_(c), provided that at least one of the radicals R_(i) or R_(j) is not alkyl;formula KA ##STR105## where R_(n) is alkyl, cycloalkyl or aryl; p is 0, 1 or 2; and R_(o), R_(p), R_(q) and R_(r), independently of one another, are as R_(a), R_(b) and R_(c) ;formula KB ##STR106## where, X is a bond, ##STR107## R_(t) is alkyl, aryl, acyl or sulphonyl; and R_(s) is as R_(a), R_(b) and R_(c).
 8. A process for stabilizing magenta couplers and/or magenta dyes in colour-photographic materials, in which a stabilizer according to claim 1 is incorporated into the material. 